Urinary Incontinence, Stress

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Review clinical trials related to Urinary Incontinence, Stress. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Allogeneic Use of Expanded Mesenchymal Stem Cells Derived From Adipose Tissue (HC106), Female Urinary Incontinence Women Over 50 Years Old

Evaluate the feasibility and safety, obtaining initial efficacy data, of expanded allogeneic mesenchymal stem cells derived from adipose tissue (HC106) for the treatment of urinary incontinence in women over 50 years of age.

Participants needed: 60
Trial details
Phase: Phase 1Age: 50+Biological sex: FemaleType: InterventionalSponsor: Instituto de Investigación Sanitaria de la Fundación Jiménez DíazUpdated: May 1, 2025Locations: 6
Eligibility criteria

Women over 50 years old [+4]

Patients with a medical history of previous surgery for incontinence, prolapse o... [+9]

Status: Recruiting

Elastographic Assessment of Suburethral Tissue in Continent and Incontinent Women

Strain elastography (SE) will be utilized as a non-invasive imaging technique to evaluate tissue elasticity and biomechanical properties in women with stress urinary incontinence (SUI) and in continent controls. The primary aim is to determine whether SE can detect differences in paraurethral tissue stiffness between these groups. Given the established role of tissue elasticity in the pathophysiology of SUI, SE will be investigated as a potential diagnostic tool in urogynecological evaluations. This prospective cohort study will be conducted at a tertiary referral center. All participants will undergo introital two-dimensional (2D) ultrasound in the midsagittal plane at rest. SE will be performed in three predefined suburethral regions of interest (ROIs): * internal urethral orifice (IUO) level * midurethra (MU) level * external urethral orifice (EUO) level The adipose layer (AL) between the external urethral meatus and the pubic symphysis will serve as the reference tissue, representing the softest anatomical structure in the region. Descriptive and comparative statistical analyses will be conducted to assess differences in paraurethral tissue stiffness between the study groups. It is hypothesized that SE will be able to detect differences in paraurethral tissue elasticity, with SUI being associated with increased tissue compliance. The study also aims to determine whether SE can reliably distinguish between varying degrees of tissue stiffness in women with SUI and continent controls. Pathophysiological focus: The study will explore key mechanisms underlying SUI, including: * Weakened bladder neck support * Impaired urethral stabilization due to increased tissue elasticity and collagen degradation * While conventional 2D ultrasound provides anatomical information, it does not directly evaluate tissue biomechanics. In contrast, SE enables real-time visualization of tissue elasticity, offering a promising adjunct to traditional urogynecological assessment methods. Standardization and Protocol The study will follow a standardized protocol to ensure reproducibility and high-quality data. Key methodological elements include: * Minimal probe compression during introital ultrasound to avoid artifacts * Bladder emptying prior to examination to eliminate confounding effects * Carefully standardized ROI placement across all patients * Controlled image acquisition conditions to reduce variability Future Directions * Future research based on this study will aim to: * Optimize SE protocols and refine ROI placement strategies * Establish clinical cutoff values for differentiating tissue stiffness in SUI vs. continent women * Assess the long-term effects of pelvic floor muscle training (PFMT) and vaginal estrogen therapy on paraurethral biomechanics * Facilitate the integration of SE into routine urogynecological practice to support early diagnosis and personalized treatment strategies for SUI

Participants needed: 80
Trial details
Age: 18-99Biological sex: FemaleType: ObservationalSponsor: Szeged UniversityUpdated: Apr 18, 2025Locations: 1
Eligibility criteria

Clinical diagnosis of stress urinary incontinence (SUI) based on patient history...

Pelvic malignancy or history of pelvic radiation therapy [+7]

Status: Recruiting

A 3 Years Naturalistic Cohort Survey Of Virtue® Male Sling System For Male Stress Urinary Incontinence

The purpose of this study is to monitor the use of Virtue® Male Sling in a real world population and collect medical data on effectiveness and to monitor safety of Virtue® at 12 and 36 months post device implantation in men with post-prostatectomy urinary incontinence.

Participants needed: 130
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Coloplast A/SUpdated: Feb 21, 2023Locations: 13
Eligibility criteria

Implanted with the Virtue® Male Sling System

Refuses to be included in the survey or that their medical data will be used for... [+1]

Status: Recruiting

Fundación IVO Registry for Patients Undergoing Sling or Artificial Urinary Sphincter After Prostate Cancer Treatment

Stress urinary incontinence is a significant potential source of morbidity after radical prostatectomy or radiation therapy for prostate cancer. At present, artificial urinary sphincter remains the preferred therapeutic option. However, this technique is not free from complications. In an attempt to avoid such complications, male sling has been suggested for use in patients with mild degrees of stress incontinence.

Participants needed: 400
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Fundación Instituto Valenciano de OncologíaUpdated: Aug 2, 2018Locations: 1Duration: 15 Years
Eligibility criteria

The subject has agreed to be treated with the male Incontinence surgery devices [+7]

The subject has an active urinary tract infection or active skin infection in re... [+10]